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Olfactory Marker/OMP Recombinant Rabbit mAb (S-3513-32)

Olfactory marker protein,Olfactory neuronal-specific protein,OMP

价格 600.00 供应商现货 : 3-5个工作日
货号 S0B6724
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产品介绍 评论(0)

产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    Olfactory Marker/OMP
  • 分子别名

    Olfactory marker protein; Olfactory neuronal-specific protein; OMP
  • 免疫原

    Recombinant Protein
  • 细胞定位

    Cytoplasm
  • Accession

    P47874
  • 克隆号

    S-3513-32
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 反应种属 ?

    Ms, Rt
  • 阳性样本

    mouse olfactory bulb, rat olfactory bulb
  • 纯化方式

    Protein A
  • 浓度

    0.25 mg/ml
  • 标记

    Unconjugated
  • 性状

    Liquid
  • 缓冲体系

    PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300

  • 储存条件

    12 months from date of receipt / reconstitution, -20 °C as supplied

  • 应用

    IHC-P ?

    WB

    IF ?

  • 稀释度

    应用 稀释度 推荐种属
    WB 1:1000 Ms, Rt
    IHC-P 1:1000 Ms, Rt
    IF 1:250 Ms, Rt
背景介绍
  • Olfactory Marker Protein (OMP) is a small, ~19 kDa cytosolic protein uniquely and abundantly expressed in mature olfactory receptor neurons (ORNs) across the vertebrate olfactory epithelium, from the cell soma to the distal axon terminals in the olfactory bulb, where it was first discovered by Frank Margolis in the 1970s as a specific molecular signature for terminally differentiated olfactory neurons. Although its precise physiological function remains incompletely understood, OMP is believed to modulate olfactory signal transduction by interacting with odorant receptor signaling cascades, regulating cAMP kinetics, and potentially facilitating odorant adaptation, while also playing roles in axon guidance, synaptic targeting, and the refinement of olfactory maps during development and regeneration. As the definitive immunohistochemical marker for mature ORNs, OMP distinguishes fully differentiated neurons from immature (expressing GAP43) and sustentacular cells, making it indispensable for studying neuronal turnover, lesion-induced regeneration, and the functional anatomy of the olfactory system in both normal and pathological states, including neurodegenerative diseases and post-viral olfactory dysfunction.

  • 免疫印迹

    • WB result of Olfactory Marker/OMP Recombinant Rabbit mAb
      Primary antibody: Olfactory Marker/OMP Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: NIH/3T3 whole cell lysate 20 µg
      Lane 2: RAW264.7 whole cell lysate 20 µg
      Lane 3: Neuro-2a whole cell lysate 20 µg
      Lane 4: mouse spleen lysate 20 µg
      Lane 5: mouse kidney lysate 20 µg
      Lane 6: mouse heart lysate 20 µg
      Lane 7: mouse brain lysate 20 µg
      Lane 8: mouse olfactory bulb lysate 20 µg
      Negative control: NIH/3T3 whole cell lysate; RAW264.7 whole cell lysate; Neuro-2a whole cell lysate; mouse spleen lysate; mouse kidney lysate; mouse heart lysate; mouse brain lysate
      Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 19 kDa
      Observed MW: 21 kDa

    • WB result of Olfactory Marker/OMP Recombinant Rabbit mAb
      Primary antibody: Olfactory Marker/OMP Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: PC-12 whole cell lysate 20 µg
      Lane 2: C6 whole cell lysate 20 µg
      Lane 3: rat kidney lysate 20 µg
      Lane 4: rat olfactory bulb lysate 20 µg
      Negative control: PC-12 whole cell lysate; C6 whole cell lysate; rat kidney lysate
      Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 19 kDa
      Observed MW: 21 kDa

  • 免疫组化

    • IHC shows positive staining in paraffin-embedded mouse olfactory bulb. Anti-Olfactory marker/OMP antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • Negative control: IHC shows negative staining in paraffin-embedded mouse spleen. Anti-Olfactory marker/OMP antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded rat olfactory bulb. Anti-Olfactory marker/OMP antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • Negative control: IHC shows negative staining in paraffin-embedded rat cerebral cortex. Anti-Olfactory marker/OMP antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

  • 免疫荧光

    • IF shows positive staining in paraffin-embedded mouse olfactory bulb. Anti-Olfactory Marker/OMP antibody was used at 1/250 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • IF shows negative staining in paraffin-embedded mouse cerebral cortex. Anti-Olfactory Marker/OMP antibody was used at 1/250 dilution and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • IF shows positive staining in paraffin-embedded rat olfactory bulb. Anti-Olfactory Marker/OMP antibody was used at 1/250 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • IF shows negative staining in paraffin-embedded rat cerebral cortex. Anti-Olfactory Marker/OMP antibody was used at 1/250 dilution and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

  • 组织表达图谱

    • Expression of Olfactory marker/OMP in mouse & rat tissues.

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